ALK and crizotinib: after the honeymoon…what else? Resistance mechanisms and new therapies to overcome it
Rolfo C(1), Passiglia F(1), Castiglia M(1), Raez LE(1), Germonpre P(1), Gil-Bazo I(1), Zwaenepoel K(1), De Wilde A(1), Bronte G(1), Russo A(1), Van Meerbeeck JP(1), Van Schil P(1), Pauwels P(1).
(1)  Phase I-Early Clinical Trials Unit, Oncology Department and Multidisciplinary Oncology Center Antwerp (MOCA), Antwerp University Hospital, Edegem, Belgium ;  Department of Surgical, Oncological and Oral Sciences, Section of Medical Oncology, University of Palermo, Palermo, Italy ;  Molecular Pathology Unit, Pathology Department, Antwerp University Hospital, Edegem, Belgium ;  Memorial Cancer Institute, Memorial Health Care System, Florida International University, Miami, FL, USA ;  Thoracic Oncology Unit, Integrated Cancer Centre, AZ Maria Middelares, Gent, Belgium ;  Lung Cancer Unit, Department of Oncology, Clinica Universidad de Navarra, Pamplona, Spain ;  Thoracic Oncology, Multidisciplinary Oncology Center Antwerp (MOCA), Antwerp University Hospital, Edegem, Belgium ;  Thoracic Surgery Department, Antwerp University Hospital, Edegem, Belgium.
Revista: Translational Lung Cancer Research
Fecha: 01/08/2014Oncología Médica
The last few decades have witnessed a silent revolution in the war against NSCLC, thanks to the discovery of "oncogenic drivers" and the subsequent development of targeted therapies.
The discovery of the EML4-ALK fusion gene in a subgroup of patients with NSCLC and the subsequent clinical development of crizotinib has been an amazing success story in lung cancer translational-research, and its accelerated approval [only 4 years from the discovery of ALK rearrangement in NSCLC to the approval by the Food and Drug Administration (FDA)] marked the beginning of the new decade of targeted therapy. However, common to all targeted therapies, despite an initial benefit, patients inevitably experience tumor progression, due to the development of resistance. Several molecular mechanisms are responsible for acquired resistance, such as secondary mutations of ALK kinase domain or amplification of ALK fusion gene, or the activation of other oncogenic drivers, which may cause resistance independently of ALK genetic alterations.
Pre-clinical data and early clinical trials showed the promising efficacy of a new class of ALK-inhibitors in overcoming acquired resistance.The inhibition of the molecular chaperone, HSP90, represents another promising strategy to overcome crizotinib resistance in ALK-rearranged NSCLC. Several molecules are currently under investigation in order to establish their specific role in the treatment of ALK-rearranged NSCLC.
CITA DEL ARTÍCULO Transl Lung Cancer Res. 2014 Aug;3(4):250-61. doi: 10.3978/j.issn.2218-6751.2014.03.01.
tal vezLE INTERESE
La Clínica es el hospital privado con mayor dotación tecnológica de España, todo en un único centro.
Los profesionales de la Clínica realizan una labor continuada de investigación y formación, siempre en beneficio del paciente.
Conozca por qué somos diferentes a otros centros sanitarios. Calidad, rapidez, comodidad y resultados.